chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	173939816	173939816		A	36	GENIC	homozygous	135961021
2	173940445	173940445		T	43	GENIC	possibly homozygous	135961022
2	173941915	173941916	A	G	74	GENIC	homozygous	136372588
2	173943800	173943801	G		51	GENIC	homozygous	135961023
2	173944287	173944288	C		42	GENIC	homozygous	135961024
2	173948550	173948551	C	T	48	GENIC	homozygous	136372592
2	173954178	173954179	T	A	73	GENIC	homozygous	136372606
2	173956071	173956072	T		18	GENIC	homozygous	403027860
2	173942907	173942908	A		12	GENIC	heterozygous	403027858
2	173942907	173942908	A	C	12	GENIC	heterozygous	403027859
2	173947140	173947141	T	A	18	GENIC	heterozygous	404507225
2	173947136	173947137	T	A	11	GENIC	homozygous	144333937
2	173947138	173947139	T	A	18	GENIC	heterozygous	144333938
2	173948931	173948933	GC		47	GENIC	homozygous	141334163
2	173951622	173951622		T	41	GENIC	possibly homozygous	141334164
2	173950913	173950914	G	A	34	GENIC	homozygous	141422228
2	173956071	173956072	T	C	18	GENIC	heterozygous	403027861
2	173956073	173956074	T	C	18	GENIC	homozygous	141422229
2	173956827	173956828	C	T	57	GENIC	homozygous	141422230